Colon Cancer: Gene >> DBF4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315005
Start	44741383:44741383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774436262
CDS Mutation	c.761C>A
AA Mutation	p.Ser254Tyr(p.S254Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315005
Start	44722973:44722973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176C>T
AA Mutation	p.Ala59Val(p.A59V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315005
Start	44750817:44750817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412A>G
AA Mutation	p.Glu471Gly(p.E471G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315005
Start	44751209:44751209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1804C>G
AA Mutation	p.Gln602Glu(p.Q602E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000315005
Start	44748465:44748465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753649695
CDS Mutation	c.1189G>A
AA Mutation	p.Val397Met(p.V397M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315005
Start	44722997:44722997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139442134
CDS Mutation	c.200C>T
AA Mutation	p.Thr67Met(p.T67M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315005
Start	44750808:44750808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146661795
CDS Mutation	c.1403C>T
AA Mutation	p.Ser468Leu(p.S468L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315005
Start	44750907:44750907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765334573
CDS Mutation	c.1502C>T
AA Mutation	p.Pro501Leu(p.P501L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315005
Start	44750863:44750863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1458G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315005
Start	44748455:44748455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315005
Start	44738398:44738398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749986101
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315005
Start	44729943:44729943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769717083
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000315005
Start	44729959:44729959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>T
AA Mutation	p.Glu94Ter(p.E94*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000315005
Start	44750726:44750726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321C>T
AA Mutation	p.Gln441Ter(p.Q441*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DBF4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315005
Start	44747172:44747172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920C>A
AA Mutation	p.Ala307Asp(p.A307D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript